Cite
HARVARD Citation
Marchet, S. et al. (2020). Homozygous mutations in C1QBP as cause of progressive external ophthalmoplegia (PEO) and mitochondrial myopathy with multiple mtDNA deletions. Human mutation. 41 (10), pp. 1745-1750. [Online].
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Marchet, S. et al. (2020). Homozygous mutations in C1QBP as cause of progressive external ophthalmoplegia (PEO) and mitochondrial myopathy with multiple mtDNA deletions. Human mutation. 41 (10), pp. 1745-1750. [Online].